Collaborative Research: Theory and Synthesis of Strained Cyclic Photoswitches Towards Controlling Isomerization and Cycloadditions

NSF Award Search · 01002526DB NSF RESEARCH & RELATED ACTIVIT · $271,019 · view on nsf.gov ↗

Abstract

With the support of the Chemical Mechanism, Function, and Properties Program of the Division of Chemistry, Professor Michael Kienzler of the Department of Chemistry at the University of Connecticut and Professor Steven Lopez of the Department of Chemistry at Northeastern University are collaborating across synthetic and theoretical chemistry to study the reactivity of molecular photoswitches. Molecular photoswitches use light to trigger controllable changes in molecular function. In this project, the PIs are using ring strain as a second means of controlling and enhancing the photoswitching functions. Using ring-strain to increase molecule reactivity is well-established in chemistry. This proposal combines these two ideas to develop cyclized photoswitches to generate ring-strain reversibly and study the activation of functional groups in the rings for wavelength-dependent spatiotemporal control of target reactions. Results from this research project will significantly impact organic chemistry, energy storage, biophysics, and chemical biology. Furthermore, this interdisciplinary project includes a substantial educational framework for supporting STEM students from high school through graduate level chemistry. The long-term goal of this collaboration is to understand the photophysical effects of ring-strain on photoswitches and to demonstrate that the reversible generation of ring-strain can accelerate otherwise unfavorable photochemical reactions. Molecular photoswitches re

Key facts

NSF award ID
2453552
Awardee
University of Connecticut (CT)
SAM.gov UEI
WNTPS995QBM7
PI
Michael A Kienzler
Primary program
01002526DB NSF RESEARCH & RELATED ACTIVIT
All programs
Estimated total
$271,019
Funds obligated
$271,019
Transaction type
Standard Grant
Period
09/01/2025 → 08/31/2028